rs886039653

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(G;G)	0	common in clinvar

Make rs886039653(A;A)

Make rs886039653(A;G)

Reference

GRCh38.p7 38.3/149

Chromosome

16

Position

78164182

Gene

WWOX

is a	snp
is	mentioned by
dbSNP	rs886039653
dbSNP (classic)	rs886039653
ClinGen	rs886039653
ebi	rs886039653
HLI	rs886039653
Exac	rs886039653
Gnomad	rs886039653
Varsome	rs886039653
LitVar	rs886039653
Map	rs886039653
PheGenI	rs886039653
Biobank	rs886039653
1000 genomes	rs886039653
hgdp	rs886039653
ensembl	rs886039653
geneview	rs886039653
scholar	rs886039653
google	rs886039653
pharmgkb	rs886039653
gwascentral	rs886039653
openSNP	rs886039653
23andMe	rs886039653
SNPshot	rs886039653
SNPdbe	rs886039653
MSV3d	rs886039653
GWAS Ctlg	rs886039653

Max Magnitude

0

ClinVar
Risk	rs886039653(A;A)
Alt	rs886039653(A;A)
Reference	Rs886039653(G;G)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	WWOX
CLNDBN	not provided
Reversed	0
HGVS	NC_000016.9:g.78198079G>A
CLNSRC
CLNACC	RCV000255229.1,